Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs593698
WTAPP1
1.000 0.040 11 102833745 intron variant G/A snv 0.10 2
rs605949
WTAPP1
1.000 0.040 11 102835016 intron variant C/T snv 0.10 2
rs569444
WTAPP1 ; MMP3
0.925 0.120 11 102836574 non coding transcript exon variant G/A;T snv 0.12; 6.7E-06 0.10 3
rs563096
MMP3 ; WTAPP1
1.000 0.040 11 102836635 non coding transcript exon variant A/T snv 0.10 2
rs655403
MMP3
1.000 0.040 11 102837776 intron variant C/T snv 0.11 2
rs646910
MMP3
1.000 0.040 11 102838791 intron variant T/A snv 0.11 2
rs566125
MMP3
1.000 0.040 11 102839740 intron variant C/T snv 0.10 3
rs476762
MMP3
1.000 0.040 11 102839976 intron variant T/A snv 0.11 2
rs680753
MMP3
1.000 0.040 11 102840850 intron variant C/G snv 0.11 2
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs678815
MMP3
0.851 0.080 11 102843046 intron variant G/A;C snv 4
rs494963
MMP3
1.000 0.040 11 102845095 upstream gene variant C/A snv 0.10 2
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs626750 1.000 0.040 11 102850214 regulatory region variant G/A snv 0.21 3
rs56184183
MMP12
1.000 0.040 11 102863081 3 prime UTR variant A/C snv 1.1E-03 1.0E-03 1
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs1422753499
MMP12
0.925 0.120 11 102873034 missense variant T/C;G snv 7.0E-06 2
rs782759740
MMP12
1.000 0.040 11 102873055 stop gained T/A;C snv 4.0E-06 1
rs371800506
MMP12
1.000 0.040 11 102873067 missense variant C/G snv 4.0E-06 1
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs10883944
STN1
1.000 0.040 10 103891899 intron variant G/T snv 0.31 2
rs1570221
STN1
1.000 0.040 10 103897116 intron variant G/A snv 0.29 1
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25